Layer-by-layer coated nanoliposomes for oral delivery of insulin
Crossing the intestinal epithelial cell barrier safely and reaching the blood with therapeutic levels of bioactive insulin have been the ultimate goal of oral insulin delivery. The optimum way to overcome the barrier lies in the design of an efficient high drug loading carrier, that can protect insu...
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sg-ntu-dr.10356-1600562022-07-12T03:49:17Z Layer-by-layer coated nanoliposomes for oral delivery of insulin Zhang, Yiming Xiong, Gordon Minru Ali, Yusuf Boehm, Bernhard Otto Huang, Yingying Venkatraman, Subbu S. School of Materials Science and Engineering Lee Kong Chian School of Medicine (LKCMedicine) Science::Medicine Colloidal Particles Chitosan Crossing the intestinal epithelial cell barrier safely and reaching the blood with therapeutic levels of bioactive insulin have been the ultimate goal of oral insulin delivery. The optimum way to overcome the barrier lies in the design of an efficient high drug loading carrier, that can protect insulin from the harsh Gastrointestinal (GI) environment and enhance its uptake and transport by epithelial cells. In the present study, we developed a multi-layered insulin loading strategy on an anionic nanoliposome surface based on electrostatic interaction with chitosan. The layer-by-layer (LbL) coated nanoliposomes achieved high insulin loading (10.7% by weight) and offered superior protection with limited release in simulated gastric fluid (SGF) (about 6% in 1 h), simulated intestinal fluid (SIF) (2% in two weeks), and phosphate buffered saline (PBS) (5% in two weeks). Intracellular imaging revealed that the LbL coated liposomes were internalized and intracellularly trafficked towards the basolateral side of the Caco-2 monolayer. Transported insulin demonstrated retention of bioactivity while crossing the epithelial barrier in the glucose uptake study in 3T3 L1-MBX adipocytes. In rat studies, oral administration of the formulation resulted in rapid absorption with a peak in plasma insulin levels 0.5 h post oral gavaging. This technology thus serves as a promising platform for potential oral insulin applications. Nanyang Technological University This work was supported by the NITHM interdisciplinary diabetes and metabolic diseases grant and HealthTech NTU ID & MDP Gap Funding. The authors would like to acknowledge interdisciplinary graduate school of Nanyang Technological University for scholarship support. 2022-07-12T03:49:17Z 2022-07-12T03:49:17Z 2021 Journal Article Zhang, Y., Xiong, G. M., Ali, Y., Boehm, B. O., Huang, Y. & Venkatraman, S. S. (2021). Layer-by-layer coated nanoliposomes for oral delivery of insulin. Nanoscale, 13(2), 776-789. https://dx.doi.org/10.1039/d0nr06104b 2040-3364 https://hdl.handle.net/10356/160056 10.1039/d0nr06104b 33295926 2-s2.0-85099780282 2 13 776 789 en Nanoscale © 2021 The Royal Society of Chemistry. All rights reserved. |
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Science::Medicine Colloidal Particles Chitosan Zhang, Yiming Xiong, Gordon Minru Ali, Yusuf Boehm, Bernhard Otto Huang, Yingying Venkatraman, Subbu S. Layer-by-layer coated nanoliposomes for oral delivery of insulin |
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Crossing the intestinal epithelial cell barrier safely and reaching the blood with therapeutic levels of bioactive insulin have been the ultimate goal of oral insulin delivery. The optimum way to overcome the barrier lies in the design of an efficient high drug loading carrier, that can protect insulin from the harsh Gastrointestinal (GI) environment and enhance its uptake and transport by epithelial cells. In the present study, we developed a multi-layered insulin loading strategy on an anionic nanoliposome surface based on electrostatic interaction with chitosan. The layer-by-layer (LbL) coated nanoliposomes achieved high insulin loading (10.7% by weight) and offered superior protection with limited release in simulated gastric fluid (SGF) (about 6% in 1 h), simulated intestinal fluid (SIF) (2% in two weeks), and phosphate buffered saline (PBS) (5% in two weeks). Intracellular imaging revealed that the LbL coated liposomes were internalized and intracellularly trafficked towards the basolateral side of the Caco-2 monolayer. Transported insulin demonstrated retention of bioactivity while crossing the epithelial barrier in the glucose uptake study in 3T3 L1-MBX adipocytes. In rat studies, oral administration of the formulation resulted in rapid absorption with a peak in plasma insulin levels 0.5 h post oral gavaging. This technology thus serves as a promising platform for potential oral insulin applications. |
author2 |
School of Materials Science and Engineering |
author_facet |
School of Materials Science and Engineering Zhang, Yiming Xiong, Gordon Minru Ali, Yusuf Boehm, Bernhard Otto Huang, Yingying Venkatraman, Subbu S. |
format |
Article |
author |
Zhang, Yiming Xiong, Gordon Minru Ali, Yusuf Boehm, Bernhard Otto Huang, Yingying Venkatraman, Subbu S. |
author_sort |
Zhang, Yiming |
title |
Layer-by-layer coated nanoliposomes for oral delivery of insulin |
title_short |
Layer-by-layer coated nanoliposomes for oral delivery of insulin |
title_full |
Layer-by-layer coated nanoliposomes for oral delivery of insulin |
title_fullStr |
Layer-by-layer coated nanoliposomes for oral delivery of insulin |
title_full_unstemmed |
Layer-by-layer coated nanoliposomes for oral delivery of insulin |
title_sort |
layer-by-layer coated nanoliposomes for oral delivery of insulin |
publishDate |
2022 |
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https://hdl.handle.net/10356/160056 |
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1738844911003762688 |